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Selective separation and recovery of Sr from environmental ions by lanthanide oxalate frameworks

Nankawa, Takuya ; Sekine, Yurina   ; Yamada, Teppei*

Among the radioisotopes to be removed, $$^{90}$$Sr, which has a radioactive half-life of 28.8 years, poses a major threat to human health and the environment because of its uptake and retention in biological systems. However, removal of $$^{90}$$Sr from wastewater is still challenging due to the difficulty of separating Sr$$^{2+}$$ from Ca$$^{2+}$$. Ca$$^{2+}$$ has a similar properties and ionic radius to $$^{90}$$Sr$$^{2+}$$. Indeed, the difference in their ionic radii is only 0.2 ${AA}$. Furthermore, the concentration of Ca$$^{2+}$$ in actual nuclear wastewater is usually much higher than that of $$^{90}$$Sr, which limits the efficient removal of $$^{90}$$Sr. Here, we developed a series of isostructural lanthanide oxalate frameworks (LOFs) comprising oxalate and eight kinds of lanthanide (Ln) ions, i.e., from Sm to Tm, for application to selective removal of $$^{90}$$Sr from wastewater using its tuned porous structure. When Tb was the host Ln of the LOF, the LOF showed extremely high Sr$$^{2+}$$ selectivity and was able to distinguish the subtle difference in ionic radius between Sr$$^{2+}$$ and Ca$$^{2+}$$. This novel pore size tuning strategy will be useful in developing custom porous materials that are easy to prepare and applicable across various fields.

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